水解酸化反应器处理高盐化工污水的优化研究

分别对平流式、折流式、升流式3种水解酸化反应器的设备运行参数进行优化,获得3种水解酸化反应器用于处理难降解高盐化工污水模拟水样的最佳设备运行参数:(1)平流式反应器搅拌器转速为150 r/min,COD(化学需氧量)去除率达到17%,VFA(挥发性脂肪酸)增长率达到167%,污水的可生化系数由0.30增大至0.42;(2)当折流式反应器导流板倾角为60°时,COD去除率为16%,VFA增长率达到83%,污水的可生化系数由0.30增大至0.40;(3)当升流式反应器内循环比为200%时,COD去除率为20%,VFA增长率达到267%,污水的可生化系数由0.30增大至0.44。试验结果表明:在这3种反应器中,采用升流式反应器所得的污泥性能和传质效率等最好的。

异位发酵解决废弃物难题

我国是猪肉消费大国,年出栏生猪7亿头,养猪业是巨大的污染源,也是巨大的有机肥料库。“常规处理方式都是耗氧发酵,也叫堆肥,但是猪场最难处理的是水分。我们这项技术,目的就是通过微生物分解发酵,让水分先蒸发,然后充分混合粪便和垫料,再进行有机肥加工。”福建农科农业发展有限公司经理叶鼎承告诉记者,这次他们是带着一项养殖粪污处理技术参加展会。叶鼎承说,按福建省年养殖生猪近2000万头推算,

Preparation of three-dimensional interconnected mesoporous anatase TiO_2-SiO_2 nanocomposites with high photocatalytic activities

In this article, we report the preparation of a three-dimensional（3D） interconnected mesoporous anatase TiO2-SiO2 nanocomposite. The nanocomposite was obtained by using an ordered two-dimensional（2D） hexagonal mesoporous anatase 70 TiO2-30 SiO2-950 nanocomposite（crystallized at 950 °C for 2 h） as a precursor, NaO H as an etchant of SiO2 via a ＂creating mesopores in the pore walls＂ approach. Our strategy adopts mild conditions of creating pores such as diluted NaO H solution, appropriate temperature and solid/liquid ratio, etc. aiming at ensuring the integrities of mesopores architecture and anatase nanocrystals. XRD, TEM and N2 sorption techniques have been used to systematically investigate the physico-chemical properties of the nanocomposites. The results show that the intrawall mesopores are highly dense and uniform（average pore size 3.6 nm）, and highly link the initial mesochannels in a 3D manner while retaining mesostructural integrity. There is no significant change to either crystallinity or size of the anatase nanocrystals before and after creating the intrawall mesopores. The photocatalytic degradation rates of rhodamine B（RhB, 0.303 min^–1） and methylene blue（MB, 0.757 min^–1） dyes on the resultant nanocomposite are very high, which are 5.1 and 5.3 times that of the precursor; even up to 16.5 and 24.1 times that of Degussa P25 photocatalyst, respectively. These results clearly demonstrate that the 3D interconnected mesopores structure plays an overwhelming role to the increments of activities. The 3D mesoporous anatase TiO2-SiO2 nanocomposite exhibits unexpected-high degradation activities to RhB and MB in the mesoporous metal oxide-based materials reported so far. Additionally, the nanocomposite is considerably stable and reusable. We believe that this method would pave the way for the preparation of other 3D highly interconnected mesoporous metal oxide-based materials with ultra-high performance.

河湾——生命的乐园

蜿蜒曲折是河流的天性,河流有了＂弯＂,就注定有了＂湾＂。河湾生物多样性水平高,具有较强的降解污染和净化水质的功能,对于保障河水的洁净、维持河流的水环境安全、调节气候具有不可替代的作用。联合国环境署2000年的权威数据表明：每公顷以河湾为代表的湿地生态系统,每年创造的价值高达14 000美元,是热带雨林的7倍,是农田的160倍。

别让湿地沦为“失地”

湿地,被称为＂地球之肾＂,覆盖地球表面仅6%,却为地球上20%的已知物种提供了生存环境。也正因为如此,它给人类和动物提供了源源不断的物质能源。

省政府办公厅关于加强湿地保护管理的通知

各市、县人民政府,省各委、办、厅、局,省各直属单位: 我省是全国湿地资源最丰富的省份之一,素有"湿地大省"之称。多年来,各级政府和有关部门在湿地保护方面做了大量工作,但由于长期以来人们对湿地生态价值认识不足。

为什么要保护地球之肾

湿地是介于陆生生态系统和水生生态系统之间的过渡性地带,是滋养世间万物重要的生态系统和生态空间,是人类可持续发展不可或缺的“小”家,更是全球多样性物种的“大”家。据记载,全球超过40%的物种都依赖湿地繁衍生息,是当之无愧的“生命摇篮”。湿地在维持生态平衡、保持生物多样性和珍稀物种资源以及涵养水源、蓄洪防旱、降解污染、调节气候、控制土壤侵蚀等方面都起到非常重要的作用.

Heterojunction between anodic TiO_2/g-C_3N_4 and cathodic WO_3/W nano-catalysts for coupled pollutant removal in a self-biased system

An anodic TiO2/g-C3N4 hetero-junction and cathodic WO3/W were used to build a self-sustained catalytic fuel cell system for oxidizing rhodamine B or triclosan and reducing NO3^--N to N2 simultaneously.The WO3 nano-catalyst was formed in situ by heating and oxidizing a tungsten wire in air.Cyclic voltammetry and current-time curves were used to characterize the electrochemical properties of the electrodes and system.Aeration and activation of molecular oxygen by self-biased TiO2/g-C3N4 led to the formation of reactive oxidizing species in the fuel cell.The mechanism of simultaneous anodic oxidation of pollutants and cathodic reduction of nitrate was proposed.The spontaneously formed circuit and tiny current were used simultaneously in treating two kinds of wastewater in the reactor chambers,even without light illumination or an external applied voltage.This new catalytic pollution control route can lower energy consumption and degrade many other kinds of pollutants.

Bicarbonate activation of hydrogen peroxide: A new emerging technology for wastewater treatment

The serious limitations of available technologies for decontamination of wastewater have compelled researchers to search for alternative solutions. Catalytic treatment with hydrogen peroxide, which appears to be one of the most efficient treatment systems, is able to degrade various organics with the help of powerful ·OH radicals. This review focuses on recent progress in the use of bicarbonate activated hydrogen peroxide for wastewater treatment. The introduction of bicarbonate to pollutant treatment has led to appreciable improvements, not only in process efficiency, but also in process stability. This review describes in detail the applications of this process in homogeneous and heterogeneous systems. The enhanced degradation, limited or lack of leaching during heterogeneous degradation, and prolonged catalysts stability during degradation are salient features of this system. This review provides readers with new knowledge regarding bicarbonate, including the fact that it does not always harm pollutant degradation, and can significantly benefit degradation under some conditions.

Peroxymonosulfate activation by Mn_3O_4/metal-organic framework for degradation of refractory aqueous organic pollutant rhodamine B

An environmentally friendly Mn‐oxide‐supported metal‐organic framework(MOF),Mn3O4/ZIF‐8,was successfully prepared using a facile solvothermal method,with a formation mechanism proposed.The composite was characterized using X‐ray diffraction,scanning electron microscopy,transmission electron microscopy,X‐ray photoelectron microscopy,and Fourier‐transform infrared spectroscopy.After characterization,the MOF was used to activate peroxymonosulfate(PMS)for degradation of the refractory pollutant rhodamine B(RhB)in water.The composite prepared at a0.5:1mass ratio of Mn3O4to ZIF‐8possessed the highest catalytic activity with negligible Mn leaching.The maximum RhB degradation of approximately98%was achieved at0.4g/L0.5‐Mn/ZIF‐120,0.3g/L PMS,and10mg/L initial RhB concentration at a reaction temperature of23°C.The RhB degradation followed first‐order kinetics and was accelerated with increased0.5‐Mn/ZIF‐120and PMS dosages,decreased initial RhB concentration,and increased reaction temperature.Moreover,quenching tests indicated that?OH was the predominant radical involved in the RhB degradation;the?OH mainly originated from SO4??and,hence,PMS.Mn3O4/ZIF‐8also displayed good reusability for RhB degradation in the presence of PMS over five runs,with a RhB degradation efficiency of more than96%and Mn leaching of less than5%for each run.Based on these findings,a RhB degradation mechanism was proposed.

Characterization of a Strain Capable of Degrading a Herbicide Mixture of Quinclorac and Bensulfuronmethyl

A bacterial strain,designated as LS,was isolated from a contaminated soil and was found to be capable of utilizing quinclorac,bensulfuronmethyl,and a mixture of the two as carbon and energy sources for growth. Strain LS was identified as Ochrobactrum sp. based on its physiological-biochemical properties,16S rDNA sequences,and phylogenetic analysis. The extent of degradation of quinclorac and bensulfuronmethyl at initial concentrations of 1.5 and 0.1 g L-1 was 90% and 67%,respectively,as measured by high performance liquid chromatography(HPLC) . When a herbicide mixture of 0.34 g L-1 quinclorac and 0.02 g L-1 bensulfuronmethyl was applied as carbon sources,quinclorac and bensulfuronmethyl were degraded at 95.7% and 67.5%,respectively. It appears that quinclorac is utilized more easily in a mixture than in a single state. The optimal temperature for growth of strain LS was 37 ℃. Strain LS grew well at pH 6 to 9 and had the highest degradation level for quinclorac and bensulfuronmethyl at an initial pH of 7 and 8,respectively. Addition of 0.25 g L-1 yeast extract could promote the growth and extent of degradation of quinclorac and bensulfuronmethyl by strain LS. Strain LS also showed the capability to degrade other aromatic compounds such as catechol,propisochlor,4-chloro-2-methylphenoxyacetic acid sodium(MCPA-Na) and imazethapy. The isolate LS shows a huge potential to be used in bioremediation for treating complex herbicide residues.

Bifunctional S-scheme g-C3N4/Bi/BiVO4 hybrid photocatalysts toward artificial carbon cycling

Although both the aerobic photocatalytic oxidation of organic pollutants into CO2 and the anaerobic photocatalytic reduction of CO2 into solar fuels have been intensively studied,few efforts have been devoted to combining these carbon-involved photocatalytic oxidation-reduction processes together,by which an artificial photocatalytic carbon cycling process can be established.The key challenge lies in the exploitation of efficient bifunctional photocatalysts,capable of triggering both aerobic oxidation and anaerobic reduction reactions.In this work,a bifunctional ternary g-C3N4/Bi/BiVO4 hybrid photocatalyst is successfully constructed,which not only demonstrates superior aerobic photocatalytic oxidation performance in degrading an organic pollutant(using the dye,Rhodamine B as a model),but also exhibits impressive photocatalytic CO2 reduction performance under anaerobic conditions.Moreover,a direct conversion of Rhodamine B to solar fuels in a one-pot anaerobic reactor can be achieved with the as-prepared ternary g-C3N4/Bi/BiVO4 hybrid photocatalyst.The excellent bifunctional photocatalytic performance of the g-C3N4/Bi/BiVO4 photocatalyst is associated with the formation of efficient S-scheme hybrid junctions,which contribute to promoting the appropriate charge dynamics,and sustaining favorable charge potentials.The formation of the S-scheme heterojunction is supported by scavenger studies and density functional theory calculations.Moreover,the in-situ formed plasmonic metallic Bi nanoparticles in the S-scheme hybrid g-C3N4/Bi/BiVO4 photocatalyst enhances vectorial interfacial electron transfer.This novel bifunctional S-scheme g-C3N4/Bi/BiVO4 hybrid photocatalyst system provides new insights for the further development of an integrated aerobic-anaerobic reaction system for photocatalytic carbon cycling.

Design of metal-organic frameworks(MOFs)-based photocatalyst for solar fuel production and photo-degradation of pollutants

Metal organic frameworks(MOFs)is a research hotspot in the solar fuel production and photo-degradation of pollutants field due to high surface area,rich metal/organic species,large pore volume,and adjustability of structures and compositions.Therefore,in this review,we first summarized the design factors of photocatalytic materials based on MOF from the perspective of"star"MOF.The modification strategies of MOFs-based photocatalysts were discussed to improve its photocatalytic activity and specific applications were summarized as well,including photocatalytic CO_(2)reduction,photocatalytic water splitting and photo-degradation of pollutants.Finally,the advantages and disadvantages of MOFs-based photocatalysts were discussed,the current challenges were highlighted,and suggestions for future research directions were proposed.

Microbial PAH-Degradation in Soil: Degradation Pathways and Contributing Factors

Adverse effects on the environment and high persistence in the microbial degradation and environmental fate of polycyclic aromatic hydrocarbons (PAHs) are motivating interest. Many soil microorganisms can degrade PAHs and use various metabolic pathways to do so. However, both the physio-chemical characteristics of compounds as well as the physical, chemical, and biological properties of soils can drastically influence the degradation capacity of naturally occurring microorganisms for field bioremediation. Modern biological techniques have been widely used to promote the efficiency of microbial PAH-degradation and make the biodegradation metabolic pathways more clear. In this review microbial degradation of PAHs in soil is discussed, with emphasis placed on the main degradation pathways and the environmental factors affecting biodegradation.

Biodegradation Kinetics of DDT in Soil under Different Environmental Conditions by Laccase Extract from White Rot Fungi

Biodegradation of 2,2-bis(p-chlorophenyl)-1,1,1-trichloroethane(DDT)in soil by laccase extract from white rot fungi under different experimental conditions was investigated.DDTs,which stands for the sum of p,p′-DDE,o,p′-DDT,p,p′-DDD and p,p′-DDT in soil was degraded efficiently,and the residue decreased rapidly during the first 15 days and then slowly during the period of 16-25 days.The biodegradation of DDTs in soil fitted the pseudo-first-order kinetics.For 5,10,15 and 25 days of incubation with laccase,the residue of DDTs in soil under different atmospheres was decreased by 20%-33%,34%-52%,41%-61%and 41%-69%respectively,under different flooding conditions that was decreased by 12%-17%,17%-30%,30%-45%and 35%-52%respectively, and for different soils that was decreased by 25%-34%,39%-53%,44%-58%and 47%-62%respectively.The half-life of DDTs in soil ranged from 15.07 to 32.95 days under O2,air or N2 atmospheres,23.07 to 40.71 days under different flooding conditions,and 18.78 to 28.88 days for different soils.Laccase is an efficient and safe agent for bioremediation of DDT-contaminated soil.

Hydrogen producing water treatment through mesoporous TiO2 nanofibers with oriented nanocrystals

The development of well-defined TiO2 nanoarchitectures is a versatile strategy to achieve high-efficiency photocatalytic performance.In this study,mesoporous TiO2 nanofibers consisting of oriented nanocrystals were fabricated by a facile vapothermal-assisted topochemical transformation of preformed H-titanate nanobelts.The vapothermal temperature is crucial in tuning the microstructures and photocatalytic redox properties of the resulting mesoporous TiO2 nanofibers.The microstructures were characterized with XRD,TEM,XPS and nitrogen adsorption-desorption isotherms,etc.The photocatalytic activities were evaluated by photocatalytic oxidation of organic pollutant(Rhodamine B as an example)as well as photocatalytic reduction of water to generate hydrogen(H2).The nanofibers vapothermally treated at 150°C showed the highest photocatalytic activity in both oxidation and reduction reactions,2 times higher than that of P25.The oriented alignment and suitable mesoporosity in the resulting nanofiber architecture were crucial for enhancing photocatalytic performances.The oriented alignment of anisotropic anatase nanocrystals shall facilitate faster vectorial charge transportation along the nanofibers architecture.And,the suitable mesoporosity and high surface area would also effectively enhance the mass exchange during photocatalytic reactions.We also demonstrate that efficient energy-recovering photocatalytic water treatments could be accomplished by a cascading oxic-anoxic process where the dye is degraded in the oxic phase and hydrogen is generated in the successive anoxic phase.This study showcases a novel and facile method to fabricate mesoporous TiO2 nanofibers with high photocatalytic activity for both clean energy production and environmental purification.

A review on TiO_2-based Z-scheme photocatalysts

TiO2‐based Z‐scheme photocatalysts have attracted considerable attention because of the low recombination rate of their photogenerated electron–hole pairs and their high photocatalytic efficiency.In this review,the reaction mechanism of Z‐scheme photocatalysts,recent research progress in the application of TiO2‐based Z‐scheme photocatalysts,and improved methods for photocatalytic performance enhancement are explored.Their applications,including water splitting,CO2reduction,decomposition of volatile organic compounds,and degradation of organic pollutants,are also described.The main factors affecting the photocatalytic performance of TiO2‐based Z‐scheme photocatalysts,such as pH,conductive medium,cocatalyst,architecture,and mass ratio,are discussed.Concluding remarks are presented,and some suggestions for the future development of TiO2‐based Z‐scheme photocatalysts are highlighted.

Comparative Bioremediation of Petroleum Hydrocarbon-Contaminated Soil by Biostimulation, Bioaugmentation and Surfactant Addition

A bench-scale biopiling experiment was conducted to hydrocarbon bioremediation in a chronically contaminated soil compare the ability of different techniques to enhance petroleum After 195 days, 10%-32% removal of TPHs （total petroleum hydrocarbons） occurred in unamended soil （control）. Biostimulation by inorganic nutrient addition enhanced TPH removal （49%） confirming that bioremediation was nutrient limited and the soil contained a well-adapted hydrocarbonoclastic microbial community. The addition of organic amendments including green waste at 25% and 50% （w/w） and a commercial product called DaramendTM had a further biostimulatory effect （50%-66%, 34%-59% and 69%-80% TPH removal respectively）. Bioaugmentation using two commercially available petroleum hydrocarbon degrading microbial cultures with nutrients enhanced TPH removal in the case of RemActivTM （60%-69%）, but had a marginal effect using Recycler 102 （49%-55%）. The effect of a non-ionic surfactant in green waste amended soil was variable （52%-72% TPH reduction）, but its potential to enhance biodegradation presumably by promoting contaminant bioavailability was demonstrated. High degradation of artificially added polycyclic aromatic hydrocarbons （PAHs） occurred after 106 days （75%-84%）, but significant differences between the control and treatments were unapparent, suggesting that spiked soils do not reflect the behavior of contaminants in genuinely polluted and weathered soil.

Dechlorination of Chlorinated Aliphatic Compounds by Micro-scale Al-Zn-Mg/Fe Powders as Advanced Zero-valent Iron

Micro-scale Al-Zn-Mg/Fe composite powders (MAF) with high reactivity and good storage properties were prepared by reducing iron onto the surface of Al-Zn-Mg alloy powders. Experimental results show that MAF as advanced zero-valent iron are highly effective for degradation of chlorinated organic compounds. The efficiency of degradation for carbon tetrachloride and perchloroethylene is higher than 99% within a period of 2 h. The efficiency of degradation for trichloroethylene by MAF after storing for one month is equivalent to that by freshly prepared nano-size zero-valent iron particles.

Interfacial engineering of graphitic carbon nitride(g-C_3N_4)-based metal sulfide heterojunction photocatalysts for energy conversion: A review

As one of the most appealing and attractive technologies, photocatalysis is widely used as a promising method to circumvent the environmental and energy problems. Due to its chemical stability and unique physicochemical, graphitic carbon nitride (g-C3N4) has become research hotspots in the community. However, g-C3N4 photocatalyst still suffers from many problems, resulting in unsatisfactory photocatalytic activity such as low specific surface area, high charge recombination and insufficient visible light utilization. Since 2009, g-C3N4-based heterostructures have attracted the attention of scientists worldwide for their greatly enhanced photocatalytic performance. Overall, this review summarizes the recent advances of g-C3N4-based nanocomposites modified with transition metal sulfide (TMS), including (1) preparation of pristine g-C3N4,(2) modification strategies of g-C3N4,(3) design principles of TMS-modified g-C3N4 heterostructured photocatalysts, and (4) applications in energy conversion. What is more, the characteristics and transfer mechanisms of each classification of the metal sulfide heterojunction system will be critically reviewed, spanning from the following categories:(1) Type I heterojunction,(2) Type II heterojunction,(3) p-n heterojunction,(4) Schottky junction and (5) Z-scheme heterojunction. Apart from that, the application of g-C3N4-based heterostructured photocatalysts in H2 evolution, CO2 reduction, N2 fixation and pollutant degradation will also be systematically presented. Last but not least, this review will conclude with invigorating perspectives, limitations and prospects for further advancing g-C3N4-based heterostructured photocatalysts toward practical benefits for a sustainable future.